Matsudaira P, Bordas J, Koch M H
Proc Natl Acad Sci U S A. 1987 May;84(10):3151-5. doi: 10.1073/pnas.84.10.3151.
Synchrotron x-ray diffraction was used to identify the oligomers that formed during the earliest stages of actin polymerization. Solution diffraction patterns from G-actin (monomer) and from F-actin (polymer) contain information about the size and shape of actin monomers and the length, width, and subunit organization of filaments. Comparison of patterns collected during polymerization reveals an increase in scatter at spacings greater than 9.0 nm; formation of scattering bands at 5.4,4.9, and 3.4 nm; formation of a scattering minimum at 6.5 nm; and the presence of an isosbestic point at 9.0 nm. These scattering bands arise from the formation of, and organization of subunits in, filaments. At various actin concentrations (0.37-5 mg/ml), the change in scatter in these regions follows simple exponential kinetics with no detectable lag. Our analysis of the x-ray patterns shows that by 0.4 sec after mixing, most of the actin has formed dimers, which then rapidly incorporate into oligomers. At 4 mg/ml the early oligomers increase in length to greater than 30.0 nm within 10 sec. These results suggest that under our conditions actin molecules condense into filaments without the rate-limiting formation of nuclei.
同步辐射X射线衍射被用于识别肌动蛋白聚合最早期阶段形成的寡聚体。来自G-肌动蛋白(单体)和F-肌动蛋白(聚合物)的溶液衍射图谱包含有关肌动蛋白单体的大小和形状以及细丝的长度、宽度和亚基组织的信息。聚合过程中收集的图谱比较显示,间距大于9.0nm时散射增加;在5.4、4.9和3.4nm处形成散射带;在6.5nm处形成散射最小值;以及在9.0nm处存在等吸收点。这些散射带源于细丝中亚基的形成和组织。在各种肌动蛋白浓度(0.37-5mg/ml)下,这些区域散射的变化遵循简单的指数动力学,没有可检测到的延迟。我们对X射线图谱的分析表明,混合后0.4秒时,大部分肌动蛋白已形成二聚体,然后迅速并入寡聚体。在4mg/ml时,早期寡聚体在10秒内长度增加到大于30.0nm。这些结果表明,在我们的条件下,肌动蛋白分子凝聚成细丝,没有核的限速形成。